المؤلفون: Christopher T. Saeui (4432354), Sagar R. Shah (5318054), Beatriz I. Fernandez-Gil (14375697), Cissy Zhang (13766053), Christian Agatemor (1488979), Kris Dammen-Brower (14375700), Mohit P. Mathew (14375703), Matthew Buettner (14375706), Prateek Gowda (5318051), Pratik Khare (14375709), Andrea Otamendi-Lopez (14375712), Shuang Yang (64650), Hui Zhang (7197), Anne Le (266801), Alfredo Quinoñes-Hinojosa (14375715), Kevin J. Yarema (104690)

مصطلحات موضوعية: Biochemistry, Cell Biology, Genetics, Physiology, Pharmacology, Cancer, Inorganic Chemistry, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, targeted metabolomics analysis, nucleotide precursor biosynthesis, new therapeutic approach, hexosamine biosynthetic pathway, growth inhibitory effects, drives multiple facets, animals tolerated 5, amino acid pools, increased metabolic flux, attenuate metabolic flux, regulated oncogenic metabolites, fold higher levels, hexosamine analogs designed, 4 , gbm cells showed, reduce flux, oncogenic properties, vivo <, reduced levels, endogenous levels, universal feature

Relation: https://figshare.com/articles/journal_contribution/Anticancer_Properties_of_Hexosamine_Analogs_Designed_to_Attenuate_Metabolic_Flux_through_the_Hexosamine_Biosynthetic_Pathway/21861762

الاتاحة: https://doi.org/10.1021/acschembio.2c00784.s001